(Q27190901)

Evernic acid (English)

10 October 2016

chemical formula

C₁₇H₁₆O₇

1 reference

Evernic acid (English)

20 November 2016

canonical SMILES

CC1=CC(=CC(=C1C(=O)OC2=CC(=C(C(=C2)C)C(=O)O)O)O)OC

1 reference

The occurrence of lichen phenolics in the xylem sap of Quercus pyrenaica, their translocation to leaves and biological significance

Evernic acid (English)

20 November 2016

1 reference

Evernia prunastri

19 references

The occurrence of lichen phenolics in the xylem sap of Quercus pyrenaica, their translocation to leaves and biological significance

High performance liquid chromatographic analysis of aliphatic lichen acids

The occurrence of lichen phenolics in the photobiont cells of Evernia prunastri

The use of urea by Evernia prunastri thalli

The lichen substances of the genus Evernia

Structure of the methyl esters of barbatic and evernic acids: natural para-depsides

Analysis of secondary metabolites from Lichen by high performance liquid chromatography with a photodiode array detector

Endogenous Inactivators of Arginase, l-Arginine Decarboxylase, and Agmatine Amidinohydrolase in Evernia prunastri Thallus

reference URL

https://dalspace.library.dal.ca/bitstream/handle/10222/77155/VOLUME%2011-NUMBERS%202-3-1991-PAGE%20345.pdf?sequence=1

182. Lichen acids. Part II. The constitution of evernic acid and the synthesis of methyl evernate

Antimicrobial and antioxidant activity of Evernia prunastri extracts and their isolates

Characterization of oakmoss products used in perfumery by high-performance liquid chromatography

A Comparative Study of Isolated Secondary Metabolites from Lichens and Their Antioxidative Properties

Structure and Chemical Analysis of Major Specialized Metabolites Produced by the Lichen Evernia prunastri

NMR assignments of depsides and tridepsides of the lichen family umbilicariaceae

Evernia prunastri and Pseudoevernia furfuraceae lichens and their major metabolites as antioxidant, antimicrobial and anticancer agents

A biochemical approach to the hemiparasitic action of the epiphytic lichen Evernia prunastri on Betula pendula

A Comparative Study of Isolated Secondary Metabolites from Lichens and Their Antioxidative Properties

Lichen Depsides and Tridepsides: Progress in Pharmacological Approaches

Ramalina calicaris

1 reference

The occurrence of lichen phenolics in the xylem sap of Quercus pyrenaica, their translocation to leaves and biological significance

Ochrolechia parella

1 reference

Some lichen products have antimicrobial activity

Pertusaria pseudocorallina

1 reference

Some lichen products have antimicrobial activity

Ramalina pollinaria

2 references

Components ofRamalina pollinaria

Chemistry of Lichen Substances

Usnea rubicunda

1 reference

Some lichen products have antimicrobial activity

Pseudevernia furfuracea

2 references

Analysis of secondary metabolites from Lichen by high performance liquid chromatography with a photodiode array detector

Lichen Depsides and Tridepsides: Progress in Pharmacological Approaches

Evernia mesomorpha

2 references

Fluorescence of Lichen Depsides and Depsidones as a Taxonomic Criterion

1 reference

Lichen Substances VII. Identification of Orsellinate Derivatives from Lobaria linita

Ramalina fastigiata

1 reference

R amalina Lichens and Their Major Metabolites as Possible Natural Antioxidant and Antimicrobial Agents

Usnea aciculifera

1 reference

A Validated HPTLC Densitometric Method for Simultaneous Determination of Evernic and Usnic Acids in Four Usnea Species and Comparison of Their Antioxidant Potential

Usnea florida

1 reference

Antibacterial activity of the lichens Usnea Florida and Flavoparmelia caperata (Parmeliaceae)

Usnea lecanorica

1 reference

A New Lecanoric Acid-Producing Usnea from Mexico

Dolichousnea longissima

2 references

Lichen acids, plant growth inhibitors from Usnea longissima

Screening of tissue cultures and thalli of lichens and some of their active constituents for inhibition of tumor promoter-induced Epstein-Barr virus activation

subject has role

antioxidant

7 references

DFT and QTAIM based investigation on the structure and antioxidant behavior of lichen substances Atranorin, Evernic acid and Diffractaic acid

Isolation, identification, thermal analysis, DFT calculations and antioxidant activity studies of lichen metabolites norstictic acid and evernic acid Abstract

Antimicrobial and antioxidant activity of Evernia prunastri extracts and their isolates

A Comparative Study of Isolated Secondary Metabolites from Lichens and Their Antioxidative Properties

A Validated HPTLC Densitometric Method for Simultaneous Determination of Evernic and Usnic Acids in Four Usnea Species and Comparison of Their Antioxidant Potential

Evernia prunastri and Pseudoevernia furfuraceae lichens and their major metabolites as antioxidant, antimicrobial and anticancer agents

A Comparative Study of Isolated Secondary Metabolites from Lichens and Their Antioxidative Properties

antimicrobial agent

6 references

Lichen secondary metabolite evernic acid as potential quorum sensing inhibitor against Pseudomonas aeruginosa.

Antifungal activity of lichen extracts and lichenic acids

Antimicrobial and antioxidant activity of Evernia prunastri extracts and their isolates

Antibacterial activity of the lichens Usnea Florida and Flavoparmelia caperata (Parmeliaceae)

Evernia prunastri and Pseudoevernia furfuraceae lichens and their major metabolites as antioxidant, antimicrobial and anticancer agents

Lichen Depsides and Tridepsides: Progress in Pharmacological Approaches

anti-inflammatory agent

1 reference

Neuroprotective and Anti-Inflammatory Effects of Evernic Acid in an MPTP-Induced Parkinson’s Disease Model

neuroprotective agent

3 references

Neuroprotective and Anti-Inflammatory Effects of Evernic Acid in an MPTP-Induced Parkinson’s Disease Model

Protective effects of lichen metabolites evernic and usnic acids against redox impairment-mediated cytotoxicity in central nervous system-like cells

Lichen Depsides and Tridepsides: Progress in Pharmacological Approaches

clastogen

1 reference

Clastogenic effect of atranorin, evernic acid, and usnic acid on human lymphocytes

antineoplastic

5 references

Antiproliferative effects on tumour cells and promotion of keratinocyte wound healing by different lichen compounds

Screening of tissue cultures and thalli of lichens and some of their active constituents for inhibition of tumor promoter-induced Epstein-Barr virus activation

Evernia prunastri and Pseudoevernia furfuraceae lichens and their major metabolites as antioxidant, antimicrobial and anticancer agents

Lecanoric acid mediates anti-proliferative effects by an M phase arrest in colon cancer cells

Lichen Depsides and Tridepsides: Progress in Pharmacological Approaches

toxicity

1 reference

Lichen Depsides and Tridepsides: Progress in Pharmacological Approaches

wound healing

1 reference

Lichen Depsides and Tridepsides: Progress in Pharmacological Approaches

Identifiers

InChI

InChI=1S/C17H16O7/c1-8-5-11(7-12(18)14(8)16(20)21)24-17(22)15-9(2)4-10(23-3)6-13(15)19/h4-7,18-19H,1-3H3,(H,20,21)

1 reference

Evernic acid (English)

20 November 2016

2 references

Evernic acid (English)

20 November 2016

ChEBI release 2020-09-01

CAS Registry Number

537-09-7

2 references

Global Substance Registration System

evernic acid (English)

20 November 2016

https://commonchemistry.cas.org/detail?cas_rn=537-09-7

8 April 2021

1 reference

2-Hydroxy-4-[(2-hydroxy-4-methoxy-6-methylbenzoyl)oxy]-6-methylbenzoic acid (English)

20 November 2016

2 references

Evernic acid (English)

20 November 2016

ChEBI ID

111284

mapping relation type

2 references

2-hydroxy-4-[(2-hydroxy-4-methoxy-6-methylphenyl)-oxomethoxy]-6-methylbenzoic acid (English)

10 October 2016

International Chemical Identifier

InChI

InChI=1S/C17H16O7/c1-8-5-11(7-12(18)14(8)16(20)21)24-17(22)15-9(2)4-10(23-3)6-13(15)19/h4-7,18-19H,1-3H3,(H,20,21)

1 reference

Mapping file of InChIStrings, InChIKeys and DTXSIDs for the EPA CompTox Dashboard

EVERNIC ACID (English)

20 November 2016

1 reference

2 references

DSSTOX compound identifier

0 references

0 references

208-658-2

1 reference

Global Substance Registration System

evernic acid (English)

ECHA Substance Infocard ID

20 November 2016

100.007.873

1 reference

ECHA Substance Infocard database

ECHA Substance Infocard ID

100.007.873

27 December 2018

4-[(4-methoxy-6-methylsalicyloyl)oxy]-6-methylsalicylic acid (English)

quotation

CAS no.: 537-09-7 (English)

2 references

Global Substance Registration System

evernic acid (English)

20 November 2016